Allele Registry

Canonical Allele Identifier: PA2826627993

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000552775

RCV002433573

RCV003398659

RCV003477462

RCV004528271

ClinVar Variation:

89321

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Tyr839Ser	CA011072 NM_001281492.2:c.2516A>C